Canonical Allele Identifier: PA915957801
Gene: RPGR HGNC NCBI

Linked Data

ClinVar Variation Id: 414013

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001030025.1:p.Thr570Ala
CA10385420
NM_001034853.2:c.1708A>G